About: Loïc Guillevin

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researcher

Attributes	Values
rdf:type	Item
description	researcher (en) 연구원 (ko) дослідник (uk) 研究者 (zh) onderzoeker (nl) médecin interniste (fr)
rdfs:label	Loïc Guillevin (de) Loïc Guillevin (en) Loïc Guillevin (es) Loïc Guillevin (fr) Loïc Guillevin (nl)
skos:prefLabel	Loïc Guillevin (de) Loïc Guillevin (en) Loïc Guillevin (es) Loïc Guillevin (fr) Loïc Guillevin (nl)
name	Loïc Guillevin (de) Loïc Guillevin (en) Loïc Guillevin (es) Loïc Guillevin (fr) Loïc Guillevin (nl)
given name	wds:Q88410079-475F3C79-9FCF-40A4-BFCC-EFE150D2E62B
given name	Loïc
instance of	wds:Q88410079-DE27F738-B95D-4A73-9634-3DBBF91217F5
instance of	Homo sapiens
occupation	wds:Q88410079-57182BE6-58E2-491C-B068-F0DE12F49DE8
employer	wds:Q88410079-1895BB6F-AE3D-4498-B6B9-02E7019DF966
NUKAT ID	wds:Q88410079-CF471459-E819-4715-94C0-B9E96310931E
sex or gender	wds:Q88410079-68368E7B-34F2-4A0D-ABFF-475FBBB5A287
VIAF ID	wds:Q88410079-89982723-6FCE-4972-986D-76AEB362C623
IdRef ID	wds:Q88410079-6728F4BC-D72F-4490-B118-745414F2BC9F
date of birth	wds:Q88410079-41AAD251-70AF-4BF5-8755-3B0AC930C13A
educated at	wds:Q88410079-6FC7462C-FA0B-4032-AB19-2EFFF6AA3696
PLWABN ID	wds:Q88410079-C179DAFB-B899-42C0-8ADD-5B9CD8C3870A
family name	wds:q88410079-21ca2f37-4aca-0617-7a53-e9761aecd964
National Library of Israel J9U ID	wds:Q88410079-6EB12286-7178-4168-95B0-E6F0D33942E8
VIAF ID	http://viaf.org/viaf/12319529
IdRef ID	http://www.idref.fr/028285840/id
occupation	researcher
employer	Hôpital Cochin
NUKAT ID	n2009150669
sex or gender	male
VIAF ID	12319529
IdRef ID	028285840
date of birth	1947-01-01 00:00:00Z (xsd:dateTime)
educated at	Pierre and Marie Curie University
PLWABN ID	9810566598405606
family name	Guillevin
National Library of Israel J9U ID	987007378752905171
ORCID iD	wds:Q88410079-25C32919-8F59-4877-A4F9-4FC039450D64
ORCID iD	https://orcid.org/0000-0001-6463-2160
ORCID iD	0000-0001-6463-2160
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q88410079
is author of	Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement Tissue-specific microvascular endothelial cells show distinct capacity to activate NK cells: implications for the pathophysiology of granulomatosis with polyangiitis Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): Clinical characteristics and long-term followup of the 383 patients enrolled in the French Vasculitis Study Group cohort Domains of health-related quality of life important to patients with giant cell arteritis Treatment of adult systemic mastocytosis with interferon-alpha: results of a multicentre phase II trial on 20 patients Valvular involvement in ANCA-associated systemic vasculitis: a case report and literature review Accumulation of hydrogen peroxide is an early and crucial step for paclitaxel-induced cancer cell death both in vitro and in vivo. Vasculitides associated with malignancies: analysis of sixty patients Hepatitis B virus-associated polyarteritis nodosa: clinical characteristics, outcome, and impact of treatment in 115 patients Pregnancies in systemic necrotizing vasculitides: report on 12 women and their 20 pregnancies New insights into the pathogenesis of systemic sclerosis Sensitivity to change in systemic sclerosis of the McMaster-Toronto Arthritis Patient Preference Disability Questionnaire (MACTAR): shift in patient priorities over time Prevalence and characteristics of moderate to severe pulmonary hypertension in systemic sclerosis with and without interstitial lung disease. Is pulmonary arterial hypertension really a late complication of systemic sclerosis? Patient preference disability questionnaire in systemic sclerosis: A cross‐sectional survey Targets of anti-endothelial cell antibodies in pulmonary hypertension and scleroderma Sjogren's syndrome is associated with and not secondary to systemic sclerosis Screening for pulmonary arterial hypertension in patients with systemic sclerosis: Clinical characteristics at diagnosis and long-term survival Bevacizumab-induced cardiovascular events: a consequence of cholesterol emboli syndrome? Induction of endothelial cell apoptosis by the binding of anti-endothelial cell antibodies to Hsp60 in vasculitis-associated systemic autoimmune diseases [Microscopic polyangiitis] Early detection of pulmonary arterial hypertension in systemic sclerosis: A French nationwide prospective multicenter study Selective oxidation of DNA topoisomerase 1 induces systemic sclerosis in the mouse. FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity Identification of target antigens of antifibroblast antibodies in pulmonary arterial hypertension. Relapsing polychondritis Reactive hemophagocytic syndrome in adult systemic disease: report of twenty-six cases and literature review Ophthalmologic manifestations of systemic necrotizing vasculitides at diagnosis: a retrospective study of 1286 patients and review of the literature. Protective effect of A/H1N1 vaccination in immune-mediated disease--a prospectively controlled vaccination study [Epidemiology of HIV-associated malignancies] Population-based prevalence study of Behçet's disease: differences by ethnic origin and low variation by age at immigration Low influenza vaccination rate among patients with systemic sclerosis. Proteinase 3 on apoptotic cells disrupts immune silencing in autoimmune vasculitis Predictors of treatment resistance and relapse in antineutrophil cytoplasmic antibody-associated small-vessel vasculitis: comparison of two independent cohorts EULAR points to consider in the development of classification and diagnostic criteria in systemic vasculitis Diagnosis and classification of eosinophilic granulomatosis with polyangiitis (formerly named Churg-Strauss syndrome). Impact of cardiac magnetic resonance imaging on eosinophilic granulomatosis with polyangiitis outcomes: A long-term retrospective study on 42 patients Eosinophilic granulomatosis with polyangiitis (Churg-Strauss) (EGPA) Consensus Task Force recommendations for evaluation and management. Prevalences of polyarteritis nodosa, microscopic polyangiitis, Wegener's granulomatosis, and Churg-Strauss syndrome in a French urban multiethnic population in 2000: a capture-recapture estimate Long-Term Outcomes Among Participants in the WEGENT Trial of Remission-Maintenance Therapy for Granulomatosis With Polyangiitis (Wegener's) or Microscopic Polyangiitis Rituximab versus azathioprine for maintenance in ANCA-associated vasculitis Revisiting the classification of clinical phenotypes of anti-neutrophil cytoplasmic antibody-associated vasculitis: a cluster analysis. Azathioprine or methotrexate maintenance for ANCA-associated vasculitis Heart transplantation in patients with eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome). Pathogenic effects of antimyeloperoxidase antibodies in patients with microscopic polyangiitis Central nervous system involvement in Wegener granulomatosis.

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